Fig. 2
From: Exploring novel MYH7 gene variants using in silico analyses in Korean patients with cardiomyopathy
Distribution of all MYH7 variants identified in this study. All variants shown are annotated according to the human genome GRCh38, using the MYH7 protein accession number NP_000248.2. Variants identified in this study are shown above the protein domain, and OMIM variants are located below. Pathogenic (P)/likely pathogenic (LP) variants reported as causal variants in ClinVar are shown in red, variants of uncertain significance (VUS) are shown in yellow, and novel variants are shown in blue. MYH7 contains functional domains such as the myosin motor, IQ, and coiled-coil domain